mt1 Melatonin Receptor in the Primate Adrenal Gland: Inhibition of Adrenocorticotropin-Stimulated Cortisol Production by Melatonin
Claudia Torres-Farfan,
Hans G. Richter,
Pedro Rojas-García,
Marcela Vergara,
María L. Forcelledo,
Luis E. Valladares,
Fernando Torrealba,
Guillermo J. Valenzuela and
María Serón-Ferré
Departamento de Ciencias Fisiológicas (C.T.-F., H.G.R., P.R.-G., M.V., M.L.F., F.T., M.S.-F.), Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Casilla 114-D, and Unidad de Biología de la Reproducción (L.E.V.), Instituto de Nutrición y Tecnología de los Alimentos, Universidad de Chile, Casilla 138-11, Santiago, Chile; and Department of Womens Health (G.J.V.), Arrowhead Regional Medical Center, Colton, California 92324
Address all correspondence and requests for reprints to: María Serón-Ferré, Departamento de Ciencias Fisiológicas, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Casilla 114-D, Santiago, Chile. E-mail: mseron{at}genes.bio.puc.cl.
The pineal hormone melatonin participates in circadian, seasonal,and reproductive physiology. The presence of melatonin bindingsites in human brain and peripheral tissues is well documented.However, in the mammalian adrenal gland, low-affinity melatoninbinding sites have been detected only in the rat by some butnot all authors. Conflicting evidence for a regulatory roleof melatonin on adrenal cortisol production, prompted us toinvestigate this possibility in a New World primate, the capuchinmonkey. Expression of melatonin receptors in the adrenal cortexwas demonstrated through pharmacological characterization andautoradiographic localization of 2-[125I]iodomelatonin bindingsites (dissociation constant = 96.9 ± 15 pM; maximalbinding capacity = 3.8 ± 0.4 fmol/mg protein). The mt1identity of these receptors was established by cDNA sequencing.Melatonin treatment of dispersed cells and explants from adrenalgland did not affect basal cortisol production. However, cortisolproduction stimulated by 100 nM ACTH was significantly inhibitedby low melatonin concentrations (0.1100 nM); this inhibitoryeffect was reversed by the mt1/MT2 melatonin antagonist luzindole.Melatonin also inhibited dibutyril-cAMP-stimulated cortisolproduction, suggesting that melatonin acts through a cAMP-independentsignaling pathway. The present data demonstrate that the primateadrenal gland cortex expresses functional mt1 melatonin receptorsand shows that melatonin inhibits ACTH-stimulated cortisol production.
This work was supported by Grants 2010140 and LíneasComplementarias 8980006, from Fondo Nacional de Desarrollo Científicoy Tecnológico, Chile, Grant 98/LABENDO/Resource MaintenanceGrant-2 from the World Health Organization, and a grant fromSan Bernardino Medical Foundation. C.T.-F. is a recipient ofa doctoral fellowship from Dirección de Investigaciónde la Pontificia Universidad Católica de Chile.
Abbreviations: Bmax, Maximum binding capacity; (Bu)2cAMP, N,O'-dibutyrylcAMP; DNase, deoxyribonuclease; GTP, guanosine 5'-triphosphate;Kd, dissociation constant; mt1 and MT2, high affinity G protein-coupledmelatonin receptors; SCN, suprachiasmatic nucleus.
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